Pleet Alexander, Sulewski Melanie, Salowe Rebecca J, Fertig Raymond, Salinas Julia, Rhodes Allison, Merritt Iii William, Natesh Vikas, Huang Jiayan, Gudiseva Harini V, Collins David W, Chavali Venkata Ramana Murthy, Tapino Paul, Lehman Amanda, Regina-Gigiliotti Meredith, Miller-Ellis Eydie, Sankar Prithvi, Ying Gui-Shuang, O'Brien Joan M
a Scheie Eye Institute , University of Pennsylvania , Philadelphia , PA , USA.
Ophthalmic Epidemiol. 2016 Aug;23(4):248-56. doi: 10.1080/09286586.2016.1193207. Epub 2016 Jun 27.
To determine the risk factors associated with progression to blindness from primary open-angle glaucoma (POAG) in an African-American population.
This study examined 2119 patients enrolled in the Primary Open-Angle African-American Glaucoma Genetics (POAAGG) study. A total of 59 eyes were identified as legally blind as a result of POAG (cases) and were age-and sex-matched to 59 non-blind eyes with glaucoma (controls). Chart reviews were performed to record known and suspected risk factors.
Cases were diagnosed with POAG at an earlier age than controls (p = 0.005). Of the 59 eyes of cases, 16 eyes (27.1%) presented with blindness at diagnosis. Cases had worse visual acuity (VA) at diagnosis (p < 0.0001), with VA worse than 20/40 conferring a 27 times higher risk of progression to blindness (p = 0.0005). Blind eyes also demonstrated more visual field defects (p = 0.01), higher pre-treatment intraocular pressure (IOP; p < 0.0001), and higher cup-to-disc ratio (p = 0.006) at diagnosis. IOP was less controlled in cases, and those with IOP ≥21 mmHg at more than 20% of follow-up visits were 73 times more likely to become blind (p < 0.0001). Cases missed a greater number of appointments per year (p = 0.003) and had non-adherence issues noted in their charts more often than controls (p = 0.03). However, other compliance data did not significantly differ between groups.
Access to care, initial VA worse than 20/40, and poor control of IOP were the major risk factors associated with blindness from POAG. Future studies should examine earlier, more effective approaches to glaucoma screening as well as the role of genetics in these significantly younger patients who progress to blindness.
确定非裔美国人原发性开角型青光眼(POAG)致盲进展的相关危险因素。
本研究对纳入原发性开角型非裔美国人青光眼遗传学(POAAGG)研究的2119例患者进行了检查。共有59只眼睛因POAG被确定为法定失明(病例组),并与59只非失明青光眼眼睛(对照组)进行年龄和性别匹配。进行病历审查以记录已知和疑似危险因素。
病例组比对照组更早被诊断为POAG(p = 0.005)。在病例组的59只眼中,16只眼(27.1%)在诊断时即已失明。病例组诊断时视力(VA)更差(p < 0.0001),VA低于20/40者致盲进展风险高27倍(p = 0.0005)。失明眼在诊断时还表现出更多的视野缺损(p = 0.01)、更高的治疗前眼压(IOP;p < 0.0001)和更高的杯盘比(p = 0.006)。病例组眼压控制较差,在超过20%的随访就诊中眼压≥21 mmHg者失明可能性高73倍(p < 0.0001)。病例组每年错过的预约次数更多(p = 0.003),病历中记录的不依从问题也比对照组更常见(p = 0.03)。然而,其他依从性数据在两组之间无显著差异。
获得医疗服务、初始VA低于20/40以及眼压控制不佳是POAG致盲的主要危险因素。未来研究应探讨更早、更有效的青光眼筛查方法以及遗传学在这些明显更年轻的致盲患者中的作用。